WHITE GLO ACTIVATED CHARCOAL TWIN PACK- sodium fluoride 
WHITE GLO USA INC

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White Glo Activated Charcoal Twin Pack toothpaste

Drug Facts

Active ingredient

Sodium monofluorophosphate 0.76% (0.1% W/V fluoride ion).

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warnings

Keep out of reach of children

under 6 years of age.

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

 Adults and children 2 years of age & older:  Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
 Children under 6 years of age:  Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.

Children under 2 years of age: Consult a dentist or doctor.

Other information

Inactive ingredients

Sorbitol, Hydrated Silica, Water, Glycerine, Sodium Lauryl Sulphate, Flavor, Charcoal, Cellulose Gum, Chondrus Crispus, Tetrasodium Pyrophosphate, Sodium Saccharin, Sodium Benzoate

Questions or comments

For customer enquiries, please contact: customer.service@whiteglo.com White Glo USA INC. 42 West Campbell Avenue, Third Floor Campbell, California 9500. www.whiteglo.com

Package Labeling:

Outer Package2
Inner Package2
WHITE GLO ACTIVATED CHARCOAL TWIN PACK 
sodium fluoride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73656-020
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-020-001 in 1 BOX10/19/2023
11 in 1 KIT; Type 1: Convenience Kit of Co-Package
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 12 TUBE 300 g
Part 1 of 1
WHITE GLO CHARCOAL 
sodium fluoride paste, dentifrice
Product Information
Item Code (Source)NDC:73656-021
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
CHONDRUS CRISPUS (UNII: OQS23HUA1X)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-021-00150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/19/2023
Labeler - WHITE GLO USA INC (117345666)

Revised: 3/2024
Document Id: 14b90660-ad22-7640-e063-6294a90a8af6
Set id: 6adaca4f-5599-41e0-9215-c7ee5c1dc372
Version: 3
Effective Time: 20240328
 
WHITE GLO USA INC